Adolescent and Young Adults Patient Bill of Rights

Cancer is tough—especially when you’re a young adult navigating an already challenging phase of life. That’s where Stupid Cancer steps in. Their mission? To end isolation and create a strong, supportive community for adolescents and young adults (AYAs) affected by cancer, including patients, survivors, caregivers, and medical professionals. Stupid Cancer believes that every AYA facing cancer deserves to be heard, informed, and empowered. Their AYA Rights Statement emphasizes key rights like access to clear medical information, fertility preservation discussions, financial guidance, and the ability to seek second opinions or switch doctors when needed. More importantly, they advocate for mental health support, peer connections, and ensuring all treatment options are available regardless of identity or background. Beyond advocacy, Stupid Cancer offers practical tips to help AYAs manage their cancer journey, from bringing a support person to medical appointments to finding an outlet for stress relief. The organization collaborates with numerous nonprofits and medical professionals to create a comprehensive support network, making sure no young person fights cancer alone. For anyone facing cancer in their teens, 20s, or 30s, Stupid Cancer is more than just a resource—it’s a movement to make cancer suck less and ensure every young patient has the tools and support they need to move forward. The Adolescent and Young Adults (AYA) Patient Bill of Rights was developed by the Stupid Cancer organisation which is based in the United States.